Yuexiandajisu E

Yuexiandajisu E
Product Name Yuexiandajisu E
CAS No.: 866556-16-3
Catalog No.: CFN92875
Molecular Formula: C20H30O5
Molecular Weight: 350.4 g/mol
Purity: >=98%
Type of Compound: Diterpenoids
Physical Desc.: Powder
Source: The herbs of Euphorbia ebracteolata
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Price:
Standard reference
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Providing storage is as stated on the product vial and the vial is kept tightly sealed, the product can be stored for up to 24 months(2-8C).

Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20C. Generally, these will be useable for up to two weeks. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour.

Need more advice on solubility, usage and handling? Please email to: service@chemfaces.com

The packaging of the product may have turned upside down during transportation, resulting in the natural compounds adhering to the neck or cap of the vial. take the vial out of its packaging and gently shake to let the compounds fall to the bottom of the vial. for liquid products, centrifuge at 200-500 RPM to gather the liquid at the bottom of the vial. try to avoid loss or contamination during handling.
  • Pharmaceuticals (Basel).2024, 17(3):341.
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  • Journal of Molecular Liquids2021, 334:116014.
  • Drug Dev Ind Pharm.2024, 50(11):938-951.
  • Applied Biological Chemistry2022, 65(77).
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  • Inflammation.2024, 02034-1.
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  • Polytechnic University of Catalonia2017, 105826
  • Pharmaceuticals.2022, 15(4), 402.
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    Planta Med. 2005 Apr;71(4):349-54.
    Cytotoxic diterpenoids from the roots of Euphorbia ebracteolata.[Pubmed: 15856412]

    METHODS AND RESULTS:
    Three new diterpenoids, yuexiandajisu D (1), Yuexiandajisu E (2) and F were isolated from the roots of Euphorbia ebracteolata, along with eight known diterpenoids, jolkinolide B (4), jolkinolide A, ent-11alpha-hydroxyabieta-8(14),13(15)-dien-16,12alpha-olide (6), ent-(13S)-hydroxyatis-16-ene-3,14-dione, ent-3beta,(13S)-dihydroxyatis-16-en-14-one, ent-3-oxokaurane-16alpha,17-diol, ent-16alpha,17-dihydroxyatisan-3-one and ent-atisane-3beta,16alpha,17-triol.
    CONCLUSIONS:
    The structures of all compounds were deduced using spectroscopic methods and confirmed for 1 and Yuexiandajisu E by single-crystal X-ray diffraction. A biogenetic pathway for the formation of 1 and Yuexiandajisu E is proposed briefly.
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